Статті в журналах з теми "Fluorogenic dyes"
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Pham, Ha H., Christopher Szent-Gyorgyi, Wendy L. Brotherton, Brigitte F. Schmidt, Kimberly J. Zanotti, Alan S. Waggoner, and Bruce A. Armitage. "Bichromophoric dyes for wavelength shifting of dye-protein fluoromodules." Organic & Biomolecular Chemistry 13, no. 12 (2015): 3699–710. http://dx.doi.org/10.1039/c4ob02522a.
Повний текст джерелаMartin, Annabell, and Pablo Rivera Fuentes. "A Baldwin-favored Cyclization Inspires the Development of Fluorogenic Polymethine Dyes for Bioimaging." CHIMIA 78, no. 4 (April 24, 2024): 196–99. http://dx.doi.org/10.2533/chimia.2024.196.
Повний текст джерелаMamaeva, Anastasiya A., Vladimir I. Martynov, Sergey M. Deyev, and Alexey A. Pakhomov. "Comparison of Colorimetric and Fluorometric Chemosensors for Protein Concentration Determination and Approaches for Estimation of Their Limits of Detection." Chemosensors 10, no. 12 (December 17, 2022): 542. http://dx.doi.org/10.3390/chemosensors10120542.
Повний текст джерелаKrell, Katja, and Hans-Achim Wagenknecht. "Fluorogenic and Bioorthogonal Modification of RNA Using Photoclick Chemistry." Biomolecules 10, no. 3 (March 21, 2020): 480. http://dx.doi.org/10.3390/biom10030480.
Повний текст джерелаMartin, Annabell, and Pablo Rivera-Fuentes. "Fluorogenic polymethine dyes by intramolecular cyclization." Current Opinion in Chemical Biology 80 (June 2024): 102444. http://dx.doi.org/10.1016/j.cbpa.2024.102444.
Повний текст джерелаLi, Chenge, Marie-Aude Plamont, Hanna L. Sladitschek, Vanessa Rodrigues, Isabelle Aujard, Pierre Neveu, Thomas Le Saux, Ludovic Jullien, and Arnaud Gautier. "Dynamic multicolor protein labeling in living cells." Chemical Science 8, no. 8 (2017): 5598–605. http://dx.doi.org/10.1039/c7sc01364g.
Повний текст джерелаBruchez, Marcel P. "Dark dyes–bright complexes: fluorogenic protein labeling." Current Opinion in Chemical Biology 27 (August 2015): 18–23. http://dx.doi.org/10.1016/j.cbpa.2015.05.014.
Повний текст джерелаQi, Jianjun, and Ching-Hsuan Tung. "Development of benzothiazole ‘click-on’ fluorogenic dyes." Bioorganic & Medicinal Chemistry Letters 21, no. 1 (January 2011): 320–23. http://dx.doi.org/10.1016/j.bmcl.2010.11.009.
Повний текст джерелаGu, Lingyue, Kévin Renault, Anthony Romieu, Jean-Alexandre Richard, and Rajavel Srinivasan. "Synthesis and spectral properties of 6′-triazolyl-dihydroxanthene-hemicyanine fused near-infrared dyes." New Journal of Chemistry 44, no. 28 (2020): 12208–15. http://dx.doi.org/10.1039/d0nj01724h.
Повний текст джерелаKarpenko, Iuliia A., Yosuke Niko, Viktor P. Yakubovskyi, Andriy O. Gerasov, Dominique Bonnet, Yuriy P. Kovtun, and Andrey S. Klymchenko. "Push–pull dioxaborine as fluorescent molecular rotor: far-red fluorogenic probe for ligand–receptor interactions." Journal of Materials Chemistry C 4, no. 14 (2016): 3002–9. http://dx.doi.org/10.1039/c5tc03411f.
Повний текст джерелаWang, Xiaoqing, Qingsong Liu, Fen Qi, Lin Li, Hai-Dong Yu, Zhipeng Liu, and Wei Huang. "Benzothiazole–pyrimidine-based BODIPY analogues: promising luminophores with fluorescence sensing and imaging ability and asymmetrization-induced solid-state emission." Dalton Transactions 45, no. 43 (2016): 17274–80. http://dx.doi.org/10.1039/c6dt03469a.
Повний текст джерелаKormos, Attila, Alexandra Egyed, Jasmine M. Olvany, Ágnes Szatmári, Adrienn Biró, Zsóka Csorba, Péter Kele, and Krisztina Németh. "A Bioorthogonal Double Fluorogenic Probe to Visualize Protein–DNA Interaction." Chemosensors 10, no. 1 (January 17, 2022): 37. http://dx.doi.org/10.3390/chemosensors10010037.
Повний текст джерелаLow, Michelle, Khin Yin Win, Enyi Ye, Shuhua Liu, Soon Huat Ng, Xiaoqun Zhou, and Ming-Yong Han. "Fluorogenic Quantification of Albumin." Australian Journal of Chemistry 67, no. 10 (2014): 1382. http://dx.doi.org/10.1071/ch14083.
Повний текст джерелаStensrud, Kenneth F., Kimberly J. Zanotti, Alan S. Waggoner, and Bruce A. Armitage. "Spectral Properties of Fluorogenic Thiophene-derived Triarylmethane Dyes." Photochemistry and Photobiology 95, no. 1 (November 23, 2018): 406–10. http://dx.doi.org/10.1111/php.13037.
Повний текст джерелаLiu, Pei, Vincent Grenier, Wootack Hong, Vikram R. Muller, and Evan W. Miller. "Fluorogenic Targeting of Voltage-Sensitive Dyes to Neurons." Journal of the American Chemical Society 139, no. 48 (November 20, 2017): 17334–40. http://dx.doi.org/10.1021/jacs.7b07047.
Повний текст джерелаSokolov, A. I., A. A. Gorshkova, N. S. Baleeva, and M. S. Baranov. "Keto-Analogs of Arylidene-Imidazolones as Fluorogenic Dyes." Russian Journal of Bioorganic Chemistry 48, no. 6 (December 2022): 1367–71. http://dx.doi.org/10.1134/s1068162022060243.
Повний текст джерелаBhasikuttan, Achikanath C., and Jyotirmayee Mohanty. "Targeting G-quadruplex structures with extrinsic fluorogenic dyes: promising fluorescence sensors." Chemical Communications 51, no. 36 (2015): 7581–97. http://dx.doi.org/10.1039/c4cc10030a.
Повний текст джерелаVasilev, Aleksey A., Meglena I. Kandinska, Stanimir S. Stoyanov, Stanislava B. Yordanova, David Sucunza, Juan J. Vaquero, Obis D. Castaño, Stanislav Baluschev, and Silvia E. Angelova. "Halogen-containing thiazole orange analogues – new fluorogenic DNA stains." Beilstein Journal of Organic Chemistry 13 (December 28, 2017): 2902–14. http://dx.doi.org/10.3762/bjoc.13.283.
Повний текст джерелаDou, Wei-Tao, Ying Lv, Chunyan Tan, Guo-Rong Chen, and Xiao-Peng He. "Irreversible destruction of amyloid fibril plaques by conjugated polymer based fluorogenic nanogrenades." Journal of Materials Chemistry B 4, no. 26 (2016): 4502–6. http://dx.doi.org/10.1039/c6tb01351a.
Повний текст джерелаAlfindee, Madher N., Yagya P. Subedi, Michelle M. Grilley, Jon Y. Takemoto, and Cheng-Wei T. Chang. "Antifungal Activities of 4″,6″-Disubstituted Amphiphilic Kanamycins." Molecules 24, no. 10 (May 16, 2019): 1882. http://dx.doi.org/10.3390/molecules24101882.
Повний текст джерелаDiana, Rosita, Barbara Panunzi, Simona Concilio, Francesco Marrafino, Rafi Shikler, Tonino Caruso та Ugo Caruso. "The Effect of Bulky Substituents on Two π-Conjugated Mesogenic Fluorophores. Their Organic Polymers and Zinc-Bridged Luminescent Networks". Polymers 11, № 9 (22 серпня 2019): 1379. http://dx.doi.org/10.3390/polym11091379.
Повний текст джерелаSmith, H. V., A. M. Grimason, C. Benton, and J. F. W. Parker. "The Occurrence of Cryptosporidium Spp. Oocysts in Scottish Waters, and the Development of a Fluorogenic Viability Assay for Individual Cryptosporidium spp. Oocysts." Water Science and Technology 24, no. 2 (July 1, 1991): 169–72. http://dx.doi.org/10.2166/wst.1991.0051.
Повний текст джерелаSilva, Gloria L., Volkan Ediz, David Yaron, and Bruce A. Armitage. "Experimental and Computational Investigation of Unsymmetrical Cyanine Dyes: Understanding Torsionally Responsive Fluorogenic Dyes." Journal of the American Chemical Society 129, no. 17 (May 2007): 5710–18. http://dx.doi.org/10.1021/ja070025z.
Повний текст джерелаQi, Jianjun, Myung-Shin Han, Yu-Cheng Chang, and Ching-Hsuan Tung. "Developing Visible Fluorogenic ‘Click-On’ Dyes for Cellular Imaging." Bioconjugate Chemistry 22, no. 9 (September 21, 2011): 1758–62. http://dx.doi.org/10.1021/bc200282t.
Повний текст джерелаKisin-Finfer, Einat, and Doron Shabat. "New repertoire of ‘donor-two-acceptor’ NIR fluorogenic dyes." Bioorganic & Medicinal Chemistry 21, no. 12 (June 2013): 3602–8. http://dx.doi.org/10.1016/j.bmc.2013.02.049.
Повний текст джерелаQi, Jianjun, and Ching-Hsuan Tung. "ChemInform Abstract: Development of Benzothiazole “Click-On” Fluorogenic Dyes." ChemInform 42, no. 20 (April 21, 2011): no. http://dx.doi.org/10.1002/chin.201120179.
Повний текст джерелаVincent, Steve, Suman Mallick, Guillaume Barnoin, Hoang-Ngoan Le, Benoît Y. Michel, and Alain Burger. "An Expeditious Approach towards the Synthesis and Application of Water-Soluble and Photostable Fluorogenic Chromones for DNA Detection." Molecules 27, no. 7 (March 31, 2022): 2267. http://dx.doi.org/10.3390/molecules27072267.
Повний текст джерелаYan, Qi, Brigitte F. Schmidt, Lydia A. Perkins, Matharishwan Naganbabu, Saumya Saurabh, Susan K. Andreko, and Marcel P. Bruchez. "Near-instant surface-selective fluorogenic protein quantification using sulfonated triarylmethane dyes and fluorogen activating proteins." Organic & Biomolecular Chemistry 13, no. 7 (2015): 2078–86. http://dx.doi.org/10.1039/c4ob02309a.
Повний текст джерелаDebieu, Sylvain, and Anthony Romieu. "In situ formation of pyronin dyes for fluorescence protease sensing." Organic & Biomolecular Chemistry 15, no. 12 (2017): 2575–84. http://dx.doi.org/10.1039/c7ob00370f.
Повний текст джерелаChi, Weijie, Lu Huang, Chao Wang, Davin Tan, Zhaochao Xu, and Xiaogang Liu. "A unified fluorescence quenching mechanism of tetrazine-based fluorogenic dyes: energy transfer to a dark state." Materials Chemistry Frontiers 5, no. 18 (2021): 7012–21. http://dx.doi.org/10.1039/d1qm00852h.
Повний текст джерелаIlieva, Sonia, Nadezhda Bozova, Miroslav Rangelov, Nadezhda Todorova, Aleksey Vasilev, and Diana Cheshmedzhieva. "Asymmetric Monomethine Cyanine Dyes with Hydrophobic Functionalities for Fluorescent Intercalator Displacement Assay." Molecules 29, no. 1 (December 23, 2023): 114. http://dx.doi.org/10.3390/molecules29010114.
Повний текст джерелаConstantin, Tudor P., Gloria L. Silva, Kelly L. Robertson, Tamara P. Hamilton, Kaitlin Fague, Alan S. Waggoner, and Bruce A. Armitage. "Synthesis of New Fluorogenic Cyanine Dyes and Incorporation into RNA Fluoromodules." Organic Letters 10, no. 8 (April 2008): 1561–64. http://dx.doi.org/10.1021/ol702920e.
Повний текст джерелаChauhan, Dinesh Pratapsinh, Tanmoy Saha, Mayurika Lahiri, and Pinaki Talukdar. "BODIPY based ‘click on’ fluorogenic dyes: application in live cell imaging." Tetrahedron Letters 55, no. 1 (January 2014): 244–47. http://dx.doi.org/10.1016/j.tetlet.2013.11.003.
Повний текст джерелаO’Connor, Liam J., Ishna N. Mistry, Sarah L. Collins, Lisa K. Folkes, Graham Brown, Stuart J. Conway, and Ester M. Hammond. "CYP450 Enzymes Effect Oxygen-Dependent Reduction of Azide-Based Fluorogenic Dyes." ACS Central Science 3, no. 1 (December 19, 2016): 20–30. http://dx.doi.org/10.1021/acscentsci.6b00276.
Повний текст джерелаZhang, Yuanwei, Xiling Yue, Bosung Kim, Sheng Yao, Mykhailo V. Bondar, and Kevin D. Belfield. "Bovine Serum Albumin Nanoparticles with Fluorogenic Near-IR-Emitting Squaraine Dyes." ACS Applied Materials & Interfaces 5, no. 17 (August 30, 2013): 8710–17. http://dx.doi.org/10.1021/am402361w.
Повний текст джерелаHo, Nan-hui, Ralph Weissleder, and Ching-Hsuan Tung. "Development of water-soluble far-red fluorogenic dyes for enzyme sensing." Tetrahedron 62, no. 4 (January 2006): 578–85. http://dx.doi.org/10.1016/j.tet.2005.10.020.
Повний текст джерелаNISHIZAWA, Seiichi, Yukina YOSHINO, Mengmeng HE, Kei HIGUCHI, Nao TOGASHI, Michiyuki SUZUKI, Yugo IGARASHI, and Yusuke SATO. "Fluorogenic Monomethine Cyanine Dyes for Nucleolar RNA Imaging in Living Cells." BUNSEKI KAGAKU 73, no. 3 (March 5, 2024): 79–86. http://dx.doi.org/10.2116/bunsekikagaku.73.79.
Повний текст джерелаChoi, Sang-Kee, Jonghoon Kim, and Eunha Kim. "Overview of Syntheses and Molecular-Design Strategies for Tetrazine-Based Fluorogenic Probes." Molecules 26, no. 7 (March 26, 2021): 1868. http://dx.doi.org/10.3390/molecules26071868.
Повний текст джерелаZanotti, Kimberly J., Gloria L. Silva, Yehuda Creeger, Kelly L. Robertson, Alan S. Waggoner, Peter B. Berget, and Bruce A. Armitage. "Blue fluorescent dye-protein complexes based on fluorogenic cyanine dyes and single chain antibody fragments." Org. Biomol. Chem. 9, no. 4 (2011): 1012–20. http://dx.doi.org/10.1039/c0ob00444h.
Повний текст джерелаDemeter, Orsolya, Attila Kormos, Christine Koehler, Gábor Mező, Krisztina Németh, Eszter Kozma, Levente B. Takács, Edward A. Lemke, and Péter Kele. "Bisazide Cyanine Dyes as Fluorogenic Probes for Bis-Cyclooctynylated Peptide Tags and as Fluorogenic Cross-Linkers of Cyclooctynylated Proteins." Bioconjugate Chemistry 28, no. 5 (April 28, 2017): 1552–59. http://dx.doi.org/10.1021/acs.bioconjchem.7b00178.
Повний текст джерелаBozhanova, Nina, Mikhail Baranov, Nadezhda Baleeva, Alexey Gavrikov, and Alexander Mishin. "Red-Shifted Aminated Derivatives of GFP Chromophore for Live-Cell Protein Labeling with Lipocalins." International Journal of Molecular Sciences 19, no. 12 (November 28, 2018): 3778. http://dx.doi.org/10.3390/ijms19123778.
Повний текст джерелаPatalag, Lukas J., and Daniel B. Werz. "Benzothiadiazole oligoene fatty acids: fluorescent dyes with large Stokes shifts." Beilstein Journal of Organic Chemistry 12 (December 14, 2016): 2739–47. http://dx.doi.org/10.3762/bjoc.12.270.
Повний текст джерелаHannig, Christian, Marie Follo, Elmar Hellwig, and Ali Al-Ahmad. "Visualization of adherent micro-organisms using different techniques." Journal of Medical Microbiology 59, no. 1 (January 1, 2010): 1–7. http://dx.doi.org/10.1099/jmm.0.015420-0.
Повний текст джерелаEdiz, Volkan, Jihoon L. Lee, Bruce A. Armitage, and David Yaron. "Molecular Engineering of Torsional Potentials in Fluorogenic Dyes via Electronic Substituent Effects." Journal of Physical Chemistry A 112, no. 40 (October 9, 2008): 9692–701. http://dx.doi.org/10.1021/jp805546s.
Повний текст джерелаKlymchenko, Andrey S. "Solvatochromic and Fluorogenic Dyes as Environment-Sensitive Probes: Design and Biological Applications." Accounts of Chemical Research 50, no. 2 (January 9, 2017): 366–75. http://dx.doi.org/10.1021/acs.accounts.6b00517.
Повний текст джерелаChen, Lei, Fei Li, Mitoshi Nandi, Lu Huang, Zhizhong Chen, Junfa Wei, Weijie Chi, Xiaogang Liu, and Jun Yang. "Towards tetrazine-based near-infrared fluorogenic dyes: Is there a wavelength limit?" Dyes and Pigments 177 (June 2020): 108313. http://dx.doi.org/10.1016/j.dyepig.2020.108313.
Повний текст джерелаCollot, Mayeul, Rémy Kreder, Anatoliy L. Tatarets, Leonid D. Patsenker, Yves Mely, and Andrey S. Klymchenko. "Bright fluorogenic squaraines with tuned cell entry for selective imaging of plasma membrane vs. endoplasmic reticulum." Chemical Communications 51, no. 96 (2015): 17136–39. http://dx.doi.org/10.1039/c5cc06094j.
Повний текст джерелаTa, Daniel D., and Sergei V. Dzyuba. "Squaraine-Based Optical Sensors: Designer Toolbox for Exploring Ionic and Molecular Recognitions." Chemosensors 9, no. 11 (October 25, 2021): 302. http://dx.doi.org/10.3390/chemosensors9110302.
Повний текст джерелаRyazantsev, Dmitry Y., Maksim V. Kvach, Dmitry A. Tsybulsky, Igor A. Prokhorenko, Irina A. Stepanova, Yury V. Martynenko, Sergey V. Gontarev, Vadim V. Shmanai, Sergey K. Zavriev, and Vladimir A. Korshun. "Design of molecular beacons: 3′ couple quenchers improve fluorogenic properties of a probe in real-time PCR assay." Analyst 139, no. 11 (2014): 2867–72. http://dx.doi.org/10.1039/c4an00081a.
Повний текст джерелаMuñoz Resta, Ignacio, and Francisco Galindo. "Phenol-based styrylpyrylium dyes for trace water detection via chromogenic and fluorogenic responses." Dyes and Pigments 197 (January 2022): 109908. http://dx.doi.org/10.1016/j.dyepig.2021.109908.
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